Canonical Allele Identifier: CA519320823

Gene: MECP2

Linked Data

• MyVariant Identifiers: chrX:g.153363084T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097627T>A , CM000685.2:g.154097627T>A	GRCh38
NC_000023.10:g.153363084T>A , CM000685.1:g.153363084T>A	GRCh37
NC_000023.9:g.153016278T>A	NCBI36
NG_007107.2:g.44495A>T
NG_007107.3:g.44477A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.-122A>T MANE Plus Clinical	ENSP00000301948.6:n.-122A>T
ENST00000453960.7:c.39A>T MANE Select	ENSP00000395535.2:p.Gly13=
ENST00000303391.10:c.-122A>T	ENSP00000301948.6:n.-122A>T
ENST00000369957.5:c.-122A>T	ENSP00000358973.4:n.-122A>T
ENST00000407218.5:c.39A>T	ENSP00000384865.2:p.Gly13=
ENST00000453960.6:c.39A>T	ENSP00000395535.2:p.Gly13=
ENST00000619732.4:c.-122A>T	ENSP00000480973.1:n.-122A>T
ENST00000627864.1:n.54A>T
ENST00000628176.2:c.-122A>T	ENSP00000486978.1:n.-122A>T
ENST00000631210.1:n.305+7154A>T
NM_001110792.1:c.39A>T	NP_001104262.1:p.Gly13=
NM_001316337.1:c.-569A>T	NP_001303266.1:n.-569A>T
NM_004992.3:c.-122A>T	NP_004983.1:n.-122A>T
XM_005274682.3:c.-513A>T	XP_005274739.1:n.-513A>T
NM_001110792.2:c.39A>T MANE Select	NP_001104262.1:p.Gly13=
NM_001316337.2:c.-569A>T	NP_001303266.1:n.-569A>T
NM_001369391.2:c.-864A>T	NP_001356320.1:n.-864A>T
NM_001369392.2:c.-513A>T	NP_001356321.1:n.-513A>T
NM_001369393.2:c.-389A>T	NP_001356322.1:n.-389A>T
NM_001386137.1:c.-794A>T	NP_001373066.1:n.-794A>T
NM_001386138.1:c.-682A>T	NP_001373067.1:n.-682A>T
NM_001386139.1:c.-558A>T	NP_001373068.1:n.-558A>T
NM_004992.4:c.-122A>T MANE Plus Clinical	NP_004983.1:n.-122A>T